Biosensor and process for producing same
a biosensor and process technology, applied in the field of biosensors, can solve the problems of inability to cope with conventional techniques, adverse effects of hematocrit level on the determination of blood glucose concentration, and inability to measure the concentration of blood glucose, and achieve the effect of high accuracy and high accuracy
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example 1
[0064]Purpose: Evaluation of gold interdigitated array electrode formed by photolithography
[0065]1. Measurement of CV value
[0066]2. Examination regarding effect of different hematocrit levels (hereinafter referred to as “Ht levels”) on sensor response:
[0067]Evaluation of gold interdigitated array electrode using Ht derived from horse blood in homogeneous solution system
[0068]Experiment:
[0069]Evaluation of gold interdigitated array electrode produced by method using mask formed by photolithography
[0070]Three gold interdigitated array electrodes (IDA) with a spacer produced by photolithography were prepared.
[0071](1) 20 μm IDA (width of working electrode / width of counter electrode / inter-electrode distance=20 μm / 20 μm / 20 μm, sum of number of working electrodes and counter electrodes=72, total area of electrode including working electrodes and counter electrodes=2.2 mm2)
[0072](2) 50 μm IDA (width of working electrode / width of counter electrode / inter-electrode distance=50 μm / 50 μm / 50 μm,...
example 2
[0095]Purpose:
[0096]1. Examination of effect of Ht on IDA electrode produced by photolithography (dry chip)
[0097]Experiment:
[0098]1. Examination of effect of Ht on IDA electrode produced by photolithography
[0099]An IDA electrode (width of working electrode / width of counter electrode / inter-electrode distance=30 μm / 30 μm, sum of number of working electrodes and counter electrodes=48, total area of electrode=2.2 mm2) with a spacer produced by photolithography was produced, and the following examination was performed.
[0100]Preserved horse blood (Nippon Biotest Laboratories Inc., Cat. No. 0103-1) was washed 5 times with PBS(−) by PBS(−) (1500 g, 10 min). To the washed blood sample, a substrate adjusted with PBS(−) so that the final concentration in the liquid component was 400 mg / dL glucose was added, whereby an Ht40 sample was prepared. The Ht40 sample was centrifuged (1000 g, 4° C., 10 min), and the resulting supernatant was added or partially removed, whereby Ht20, Ht30, Ht40, Ht50 an...
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